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首页> 外文期刊>Crop & Pasture Science >Introgression of allelic diversity from genetically distinct variants of Brassica rapa into Brassica napus canola and inheritance of the B. rapa alleles
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Introgression of allelic diversity from genetically distinct variants of Brassica rapa into Brassica napus canola and inheritance of the B. rapa alleles

机译:从芸苔属rapa的遗传明显变种转化为芸苔果酱油菜的等位基因多样性,并遗传B. Rapa等位基因

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Broadening of genetic diversity in spring oilseed Brassica napus L. (AACC, 2n = 38) canola is important for continued improvement of this crop. For this, the vast allelic diversity of theAgenome of Brassica rapa L. (AA, 2n = 20) can be utilised. We investigated the prospect of developing canola-quality euploid B. napus lines carrying the alleles of B. rapa from F-2 and BC1 (F-1 x B. napus) populations of three B. napus x B. rapa interspecific crosses involving one B. napus and three genetically distinct B. rapa parents. In meiosis, the F-1 AAC hybrid was expected to show normal segregation for the A genome chromosomes, whereas a range of C chromosomes from zero to nine was expected to be included in the gametes due to random segregation of this haploid set of chromosomes. Subsequent self-pollination, theoretically, should have eliminated the unpaired C chromosomes and resulted in a majority of B. rapa type. However, no B. rapa-type progeny were detected, and all progeny in the F-8 conformed to be B. napus type. Correlation between parent and offspring generation, grown in greenhouse or field, was weak to moderate for seed glucosinolate content; however, the simpler genetic control of this trait, involving only theAgenome loci, allowed the development of low-glucosinolate lines from this interspecific cross. Of the theoretical number of simple sequence repeat (SSR) marker alleles of B. rapa expected to be present in F-4 and F-8 populations, about 45% were detected in these populations, suggesting that the loss of these marker alleles occurred prior to the F-4 generation. Loss of several SSR loci was also detected in these populations, which probably resulted from homoeologous pairing and rearrangements of the chromosomes of the A and C genomes. Genetic diversity analysis performed on the F-8 progeny of two crosses showed that the two populations clustered into distinct groups, which demonstrates that they inherited SSR B. rapa alleles unique to each B. rapa parent. We conclude that B. rapa alleles from diverse sources can be readily incorporated into B. napus progeny by this interspecific crossing method.
机译:扩大春季油籽芸苔豆类植物中的遗传多样性L.(AACC,2N = 38)Canola对于持续改善这种作物是重要的。为此,可以利用芸苔属Rapa L.(AA,2N = 20)的巨大等位基因。我们调查了携带B.Apus x B.涉及一个涉及一个人的B.Apus x B.的燃烧室和BC1(F-1 x B. Napus)的等位基因携带B.Apa的等位基因的脱钙族蛋白质的前景。 B. Napus和三种转基因突出的B. Rapa父母。预期F-1 AAC杂种的F-1 AAC杂交物对基因组染色体显示正常的偏析,而预期从0到九的C染色体,由于这种单倍体染色体的随机偏析,在配子中包含在配子中。随后的自授粉理论上,应该消除未配对的C染色体,并导致大部分B. RAPA类型。然而,没有检测到B. Rapa型后代,并且F-8中的所有后代符合B. Napus型。在温室或场中生长的父母和后代生成之间的相关性弱于种子葡萄糖苷含量的中度;然而,这种特征的更简单的遗传控制,涉及仅仅是基因座,允许从这种间隙的十字架发育低葡糖苷系。在这些群体中预期在F-4和F-8种群中存在的B. Rapa的简单序列重复(SSR)标记等位基因的影响。在这些群体中检测到约45%,表明在之前发生了这些标记等位基因的丧失到F-4代。在这些群体中也检测到几个SSR基因座的损失,这可能是由A和C基因组染色体的同种型配对和重排。对两个十字架的F-8后代进行的遗传多样性分析表明,两种群体聚集成不同的群体,这表明它们遗传了每个B. Rapa父母独特的SSR B. Rapa等位基因。我们得出结论,来自不同来源的Rapa等位基因可以容易地通过这种间隙交叉方法纳入B. Napus后代。

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